SG188623A1 - Fluorine-containing elastomer compositions suitable for high temperature applications - Google Patents
Fluorine-containing elastomer compositions suitable for high temperature applications Download PDFInfo
- Publication number
- SG188623A1 SG188623A1 SG2013020961A SG2013020961A SG188623A1 SG 188623 A1 SG188623 A1 SG 188623A1 SG 2013020961 A SG2013020961 A SG 2013020961A SG 2013020961 A SG2013020961 A SG 2013020961A SG 188623 A1 SG188623 A1 SG 188623A1
- Authority
- SG
- Singapore
- Prior art keywords
- curable
- cure site
- perfluoropolymer
- fluorine
- composition according
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 168
- 229910052731 fluorine Inorganic materials 0.000 title claims abstract description 47
- 229920001971 elastomer Polymers 0.000 title claims abstract description 45
- 239000011737 fluorine Substances 0.000 title claims abstract description 45
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 title claims abstract description 44
- 239000000806 elastomer Substances 0.000 title claims abstract description 44
- 229920005548 perfluoropolymer Polymers 0.000 claims abstract description 188
- 239000000178 monomer Substances 0.000 claims abstract description 95
- 229920002313 fluoropolymer Polymers 0.000 claims abstract description 57
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 48
- 239000002245 particle Substances 0.000 claims abstract description 40
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims abstract description 19
- 229920006169 Perfluoroelastomer Polymers 0.000 claims description 51
- 150000001875 compounds Chemical class 0.000 claims description 48
- 238000001723 curing Methods 0.000 claims description 35
- 238000006116 polymerization reaction Methods 0.000 claims description 30
- 125000004432 carbon atom Chemical group C* 0.000 claims description 28
- 238000002156 mixing Methods 0.000 claims description 24
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 20
- 239000004811 fluoropolymer Substances 0.000 claims description 19
- 239000004816 latex Substances 0.000 claims description 15
- 229920000126 latex Polymers 0.000 claims description 15
- 229910052757 nitrogen Inorganic materials 0.000 claims description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 13
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 11
- 125000000962 organic group Chemical group 0.000 claims description 11
- 125000006551 perfluoro alkylene group Chemical group 0.000 claims description 10
- -1 cyano, carboxyl Chemical group 0.000 claims description 8
- 125000002947 alkylene group Chemical group 0.000 claims description 7
- 150000004982 aromatic amines Chemical class 0.000 claims description 7
- 238000013007 heat curing Methods 0.000 claims description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 238000007493 shaping process Methods 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 description 50
- 239000000945 filler Substances 0.000 description 28
- 239000000463 material Substances 0.000 description 27
- 238000004132 cross linking Methods 0.000 description 21
- 238000000034 method Methods 0.000 description 20
- 238000007906 compression Methods 0.000 description 18
- 230000006835 compression Effects 0.000 description 18
- 239000000126 substance Substances 0.000 description 14
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 14
- 125000003118 aryl group Chemical group 0.000 description 13
- 229920001577 copolymer Polymers 0.000 description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 12
- 125000000217 alkyl group Chemical group 0.000 description 11
- BLTXWCKMNMYXEA-UHFFFAOYSA-N 1,1,2-trifluoro-2-(trifluoromethoxy)ethene Chemical compound FC(F)=C(F)OC(F)(F)F BLTXWCKMNMYXEA-UHFFFAOYSA-N 0.000 description 10
- 239000004065 semiconductor Substances 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 9
- 125000004093 cyano group Chemical group *C#N 0.000 description 9
- 125000000524 functional group Chemical group 0.000 description 9
- 229920000728 polyester Polymers 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 8
- 238000007789 sealing Methods 0.000 description 8
- 125000003545 alkoxy group Chemical group 0.000 description 7
- 239000011258 core-shell material Substances 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 239000007767 bonding agent Substances 0.000 description 6
- 239000003431 cross linking reagent Substances 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 5
- 150000002825 nitriles Chemical class 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 125000003710 aryl alkyl group Chemical group 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- 239000011256 inorganic filler Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 125000002560 nitrile group Chemical group 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 3
- GQILCMONWYJNFP-UHFFFAOYSA-N 4-[2-(3-amino-4-anilinophenyl)-1,1,1,3,3,3-hexafluoropropan-2-yl]-1-n-phenylbenzene-1,2-diamine Chemical compound NC1=CC(C(C=2C=C(N)C(NC=3C=CC=CC=3)=CC=2)(C(F)(F)F)C(F)(F)F)=CC=C1NC1=CC=CC=C1 GQILCMONWYJNFP-UHFFFAOYSA-N 0.000 description 3
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 3
- 239000004642 Polyimide Substances 0.000 description 3
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 3
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 3
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 3
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 3
- 125000002102 aryl alkyloxo group Chemical group 0.000 description 3
- 125000004104 aryloxy group Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 3
- 150000003949 imides Chemical class 0.000 description 3
- 229910003475 inorganic filler Inorganic materials 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000011859 microparticle Substances 0.000 description 3
- 239000002105 nanoparticle Substances 0.000 description 3
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 3
- 229920001721 polyimide Polymers 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 230000009257 reactivity Effects 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 229920003051 synthetic elastomer Polymers 0.000 description 3
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 3
- CRHIAMBJMSSNNM-UHFFFAOYSA-N tetraphenylstannane Chemical compound C1=CC=CC=C1[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 CRHIAMBJMSSNNM-UHFFFAOYSA-N 0.000 description 3
- 229920001169 thermoplastic Polymers 0.000 description 3
- 239000004416 thermosoftening plastic Substances 0.000 description 3
- NFCPRRWCTNLGSN-UHFFFAOYSA-N 2-n-phenylbenzene-1,2-diamine Chemical compound NC1=CC=CC=C1NC1=CC=CC=C1 NFCPRRWCTNLGSN-UHFFFAOYSA-N 0.000 description 2
- JGMQEXIDVPFWHK-UHFFFAOYSA-N 4-[2-[3-amino-4-(methylamino)phenyl]-1,1,1,3,3,3-hexafluoropropan-2-yl]-1-n-methylbenzene-1,2-diamine Chemical compound C1=C(N)C(NC)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(NC)C(N)=C1 JGMQEXIDVPFWHK-UHFFFAOYSA-N 0.000 description 2
- IWSQPRSYFPOVBX-UHFFFAOYSA-N 4-[2-[3-amino-4-(propylamino)phenyl]-1,1,1,3,3,3-hexafluoropropan-2-yl]-1-n-propylbenzene-1,2-diamine Chemical compound C1=C(N)C(NCCC)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(NCCC)C(N)=C1 IWSQPRSYFPOVBX-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- 108700028369 Alleles Proteins 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 239000004696 Poly ether ether ketone Substances 0.000 description 2
- 239000004962 Polyamide-imide Substances 0.000 description 2
- 239000004697 Polyetherimide Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000010306 acid treatment Methods 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 150000001411 amidrazones Chemical class 0.000 description 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- JUPQTSLXMOCDHR-UHFFFAOYSA-N benzene-1,4-diol;bis(4-fluorophenyl)methanone Chemical compound OC1=CC=C(O)C=C1.C1=CC(F)=CC=C1C(=O)C1=CC=C(F)C=C1 JUPQTSLXMOCDHR-UHFFFAOYSA-N 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000013536 elastomeric material Substances 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical group FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 150000002460 imidazoles Chemical class 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000012766 organic filler Substances 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- 239000012860 organic pigment Substances 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- SIWVEOZUMHYXCS-UHFFFAOYSA-N oxo(oxoyttriooxy)yttrium Chemical compound O=[Y]O[Y]=O SIWVEOZUMHYXCS-UHFFFAOYSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- LNHURPJLTHSVMU-UHFFFAOYSA-N para-Benzoquinone dioxime Chemical compound ON=C1C=CC(=NO)C=C1 LNHURPJLTHSVMU-UHFFFAOYSA-N 0.000 description 2
- SNGREZUHAYWORS-UHFFFAOYSA-N perfluorooctanoic acid Chemical compound OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F SNGREZUHAYWORS-UHFFFAOYSA-N 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920001643 poly(ether ketone) Polymers 0.000 description 2
- 229920002312 polyamide-imide Polymers 0.000 description 2
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- 229920001601 polyetherimide Polymers 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- FYNROBRQIVCIQF-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole-5,6-dione Chemical compound C1=CN=C2C(=O)C(=O)N=C21 FYNROBRQIVCIQF-UHFFFAOYSA-N 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- KHXKESCWFMPTFT-UHFFFAOYSA-N 1,1,1,2,2,3,3-heptafluoro-3-(1,2,2-trifluoroethenoxy)propane Chemical compound FC(F)=C(F)OC(F)(F)C(F)(F)C(F)(F)F KHXKESCWFMPTFT-UHFFFAOYSA-N 0.000 description 1
- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 description 1
- BZPCMSSQHRAJCC-UHFFFAOYSA-N 1,2,3,3,4,4,5,5,5-nonafluoro-1-(1,2,3,3,4,4,5,5,5-nonafluoropent-1-enoxy)pent-1-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)=C(F)OC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)F BZPCMSSQHRAJCC-UHFFFAOYSA-N 0.000 description 1
- KGKGGKFBBFCWHG-UHFFFAOYSA-N 1-[1,2-difluoro-2-(trifluoromethoxy)ethenoxy]-1,2-difluoro-2-(trifluoromethoxy)ethene Chemical compound FC(=C(OC(F)(F)F)F)OC(=C(F)OC(F)(F)F)F KGKGGKFBBFCWHG-UHFFFAOYSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- IRPGOXJVTQTAAN-UHFFFAOYSA-N 2,2,3,3,3-pentafluoropropanal Chemical compound FC(F)(F)C(F)(F)C=O IRPGOXJVTQTAAN-UHFFFAOYSA-N 0.000 description 1
- SONQUBLFXUMJKL-UHFFFAOYSA-N 2,3-diaminobenzenethiol Chemical compound NC1=CC=CC(S)=C1N SONQUBLFXUMJKL-UHFFFAOYSA-N 0.000 description 1
- MGTZNGICWXYDPR-ZJWHSJSFSA-N 3-[[(2r)-2-[[(2s)-2-(azepane-1-carbonylamino)-4-methylpentanoyl]amino]-3-(1h-indol-3-yl)propanoyl]amino]butanoic acid Chemical compound N([C@@H](CC(C)C)C(=O)N[C@H](CC=1C2=CC=CC=C2NC=1)C(=O)NC(C)CC(O)=O)C(=O)N1CCCCCC1 MGTZNGICWXYDPR-ZJWHSJSFSA-N 0.000 description 1
- OPQNRHUSFJZWAU-UHFFFAOYSA-N 4-(1,1,1,3,3,3-hexafluoropropan-2-yl)benzene-1,3-diamine Chemical compound NC1=C(C=CC(=C1)N)C(C(F)(F)F)C(F)(F)F OPQNRHUSFJZWAU-UHFFFAOYSA-N 0.000 description 1
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- 150000002976 peresters Chemical class 0.000 description 1
- RVZRBWKZFJCCIB-UHFFFAOYSA-N perfluorotributylamine Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)N(C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F RVZRBWKZFJCCIB-UHFFFAOYSA-N 0.000 description 1
- 150000004968 peroxymonosulfuric acids Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001652 poly(etherketoneketone) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920000412 polyarylene Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920000307 polymer substrate Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 238000011417 postcuring Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000003847 radiation curing Methods 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000010057 rubber processing Methods 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 229920006126 semicrystalline polymer Polymers 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- HIFJUMGIHIZEPX-UHFFFAOYSA-N sulfuric acid;sulfur trioxide Chemical compound O=S(=O)=O.OS(O)(=O)=O HIFJUMGIHIZEPX-UHFFFAOYSA-N 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000006276 transfer reaction Methods 0.000 description 1
- SBXWFLISHPUINY-UHFFFAOYSA-N triphenyltin Chemical compound C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 SBXWFLISHPUINY-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Classifications
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/22—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
- C08F214/18—Monomers containing fluorine
- C08F214/26—Tetrafluoroethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C08K5/18—Amines; Quaternary ammonium compounds with aromatically bound amino groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08L27/18—Homopolymers or copolymers or tetrafluoroethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2500/00—Characteristics or properties of obtained polyolefins; Use thereof
- C08F2500/21—Rubbery or elastomeric properties
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
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- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
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US38646510P | 2010-09-24 | 2010-09-24 | |
PCT/US2011/052424 WO2012040250A2 (en) | 2010-09-24 | 2011-09-20 | Fluorine-containing elastomer compositions suitable for high temperature applications |
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US (1) | US9018309B2 (ja) |
EP (1) | EP2619267A4 (ja) |
JP (1) | JP5833657B2 (ja) |
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SG (1) | SG188623A1 (ja) |
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---|---|---|---|---|
US9365712B2 (en) | 2010-09-24 | 2016-06-14 | Greene, Tweed Technologies, Inc. | Fluorine-containing elastomer compositions suitable for high temperature applications |
WO2014066268A2 (en) | 2012-10-22 | 2014-05-01 | Greene, Tweed Of Delaware, Inc. | Cross-linked organic polymer compositions and methods for controlling cross-linking reaction rate and of modifying same to enhance processability |
JP6272908B2 (ja) | 2013-01-28 | 2018-01-31 | デルスパー リミテッド パートナーシップ | シーリングおよび耐摩耗性構成部材のための抗押出性組成物 |
US9109075B2 (en) | 2013-03-15 | 2015-08-18 | Delsper LP | Cross-linked organic polymers for use as elastomers in high temperature applications |
WO2014179432A1 (en) * | 2013-05-02 | 2014-11-06 | 3M Innovative Properties Company | Partially fluorinated elastomers and methods of making and using thereof |
MY186034A (en) * | 2013-08-09 | 2021-06-15 | Shawcor Ltd | High temperature insulated pipelines |
JP6230415B2 (ja) * | 2013-12-27 | 2017-11-15 | 日本バルカー工業株式会社 | パーフルオロエラストマー組成物、並びにシール材及びその製造方法 |
KR102299308B1 (ko) * | 2014-01-22 | 2021-09-07 | 그린, 트위드 테크놀로지스, 인코포레이티드 | 고온용에 적합한 불소-함유 엘라스토머 조성물 |
JP6871176B2 (ja) | 2015-05-29 | 2021-05-12 | スリーエム イノベイティブ プロパティズ カンパニー | オキサゾールを含むペルフルオロエラストマー組成物 |
CN108350244B (zh) | 2015-10-23 | 2021-01-29 | 3M创新有限公司 | 包含无定形含氟聚合物和氟塑料粒子的组合物及其制备方法 |
JP6955384B2 (ja) * | 2016-07-13 | 2021-10-27 | 株式会社バルカー | パーフルオロエラストマー組成物及びシール材 |
CN111801383A (zh) * | 2018-02-12 | 2020-10-20 | 索尔维特殊聚合物意大利有限公司 | 氟弹性体可固化的组合物 |
JP7248402B2 (ja) * | 2018-09-26 | 2023-03-29 | スリーエム イノベイティブ プロパティズ カンパニー | 硬化性フッ素系エラストマーコンポジット及びその硬化物 |
JP7155286B2 (ja) * | 2018-12-04 | 2022-10-18 | 株式会社バルカー | エラストマー組成物及びシール材 |
US20210179804A1 (en) * | 2019-08-26 | 2021-06-17 | Greene, Tweed Technologies, Inc. | Fluorine-Containing Elastomer Compositions Including Microdiamond |
CN115210300A (zh) * | 2020-03-25 | 2022-10-18 | Agc株式会社 | 复合粒子、复合粒子的制造方法、液态组合物、层叠体的制造方法及膜的制造方法 |
JP7160227B2 (ja) | 2020-04-13 | 2022-10-25 | Agc株式会社 | 含フッ素共重合体組成物および架橋ゴム物品 |
WO2021210503A1 (ja) | 2020-04-13 | 2021-10-21 | Agc株式会社 | 含フッ素共重合体組成物および架橋ゴム物品 |
WO2022125666A1 (en) * | 2020-12-08 | 2022-06-16 | Greene, Tweed Technologies, Inc. | Polymer and elastomer compositions having carbon nanostructure additives and articles formed therefrom for use in emi and rfi shielding and in pressure sensing seals having quantum tunneling composite effects |
EP4324861A1 (en) | 2021-04-12 | 2024-02-21 | Agc Inc. | Fluorocopolymer, method for producing fluorocopolymer, fluorocopolymer composition, and crosslinked rubber article |
CN116751428A (zh) * | 2023-08-23 | 2023-09-15 | 上海森桓新材料科技有限公司 | 一种高温低压缩永久变形全氟醚弹性体组合物的制备方法 |
Family Cites Families (65)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1145445A (en) | 1966-02-16 | 1969-03-12 | Du Pont | Fluorinated perfluorovinylethers, their preparation and copolymers thereof |
US3484503A (en) | 1967-06-19 | 1969-12-16 | Du Pont | Blends of fluorinated polymers |
US3723577A (en) | 1970-11-05 | 1973-03-27 | Minnesota Mining & Mfg | Fluorinated elastomer blends |
US4281092A (en) | 1978-11-30 | 1981-07-28 | E. I. Du Pont De Nemours And Company | Vulcanizable fluorinated copolymers |
US4413094A (en) | 1982-09-29 | 1983-11-01 | E. I. Du Pont De Nemours & Co. | Perfluoroelastomer blends |
US4469846A (en) * | 1983-05-20 | 1984-09-04 | E. I. Du Pont De Nemours And Company | Core/shell fluoropolymer compositions |
US4713418A (en) | 1985-12-06 | 1987-12-15 | E. I. Du Pont De Nemours And Company | Blends of fluoroplastics and fluoroelastomers |
US5260351A (en) | 1989-04-24 | 1993-11-09 | E. I. Du Pont De Nemours And Company | Radiation curing of perfluoroelastomers |
DE606883T1 (de) | 1993-01-14 | 1995-03-16 | Nippon Mektron Kk | Fluorhaltige Elastomermischung. |
JP3307046B2 (ja) | 1993-12-29 | 2002-07-24 | ダイキン工業株式会社 | フッ素ゴム組成物および成形品 |
US5447993A (en) | 1994-04-19 | 1995-09-05 | E. I. Du Pont De Nemours And Company | Perfluoroelastomer curing |
US5824749A (en) | 1994-10-04 | 1998-10-20 | Nippon Mektron, Limited | Fluorine-containing elastomer composition |
JP2833645B2 (ja) | 1994-10-21 | 1998-12-09 | 日本メクトロン株式会社 | 含フッ素エラストマー組成物 |
JPH08119931A (ja) | 1994-10-21 | 1996-05-14 | Nippon Mektron Ltd | ビスアミノチオフェノール化合物 |
JP3398492B2 (ja) | 1994-10-21 | 2003-04-21 | 日本メクトロン株式会社 | 含フッ素エラストマー組成物 |
JP3171826B2 (ja) | 1994-10-21 | 2001-06-04 | 日本メクトロン株式会社 | 含フッ素エラストマー |
JPH08143535A (ja) | 1994-11-17 | 1996-06-04 | Nippon Mektron Ltd | ビスアミノチオフェノール化合物、その製造法およびそれよりなる含フッ素エラストマー用硬化剤 |
JP2770769B2 (ja) | 1995-02-16 | 1998-07-02 | 日本メクトロン株式会社 | ビスアミドキシム化合物、その製造法およびそれを含有する含フッ素エラストマー組成物 |
JP2891294B2 (ja) | 1995-07-13 | 1999-05-17 | 日本メクトロン株式会社 | 含フッ素エラストマー組成物 |
JP3082626B2 (ja) | 1995-07-19 | 2000-08-28 | 日本メクトロン株式会社 | 含フッ素エラストマー組成物 |
US5696189A (en) | 1995-12-01 | 1997-12-09 | E. I. Du Pont De Nemours And Company | Perfluoroelastomer compositions |
US5677389A (en) | 1996-11-25 | 1997-10-14 | E. I. Du Pont De Nemours | Perfluoroelastomer composition having enhanced curing performance |
US5936060A (en) | 1996-11-25 | 1999-08-10 | E. I. Du Pont De Nemours And Company | Perfluoroelastomer composition having improved processability |
US5874523A (en) | 1996-11-25 | 1999-02-23 | E. I. Du Pont De Nemours And Company | Sulfonated perfluoroelastomer composition having improved processability |
IT1301780B1 (it) | 1998-06-23 | 2000-07-07 | Ausimont Spa | Fluoroelastomeri vulcanizzabili per via perossidica |
RU2137781C1 (ru) | 1998-08-05 | 1999-09-20 | Государственное унитарное предприятие "Научно-исследовательский институт синтетического каучука им.акад.С.В.Лебедева" | Сополимеры тетрафторэтилена и перфторалкилвиниловых эфиров для термоагрессивостойких изделий |
JP4602555B2 (ja) | 1998-11-13 | 2010-12-22 | ダイキン工業株式会社 | 含フッ素エラストマーおよびその架橋用組成物 |
IT1308627B1 (it) | 1999-02-23 | 2002-01-09 | Ausimont Spa | Composizioni fluoroelastomeriche. |
IT1308628B1 (it) | 1999-02-23 | 2002-01-09 | Ausimont Spa | Composizioni fluoroelastomeriche. |
US6518366B1 (en) | 1999-03-31 | 2003-02-11 | Daikin Industries, Ltd. | Nitrile group-containing fluoroelastomer and preparation process of same |
US6756445B1 (en) | 1999-09-30 | 2004-06-29 | Daikin Industries, Ltd. | Transparent elastomer composition |
WO2001032773A1 (fr) | 1999-11-04 | 2001-05-10 | Daikin Industries, Ltd. | Composition a base d'elastomere fluore pour reticulation |
US6638999B2 (en) | 2000-02-08 | 2003-10-28 | Dupont Dow Elastomers Llc. | Curable perfluoroelastomer composition |
JP2002012727A (ja) | 2000-04-25 | 2002-01-15 | Nippon Mektron Ltd | 含フッ素エラストマー組成物 |
JP4505957B2 (ja) | 2000-06-27 | 2010-07-21 | ダイキン工業株式会社 | 架橋用エラストマー組成物 |
US6737479B2 (en) | 2000-11-17 | 2004-05-18 | Immix Technologies, Llc | Dynamically cured fluoroelastomer blends |
US6730760B2 (en) | 2001-01-31 | 2004-05-04 | 3M Innovative Properties Company | Perfluoroelastomers having a low glass transition temperature and method of making them |
US6890995B2 (en) | 2001-01-31 | 2005-05-10 | 3M Innovative Properties Company | Fluoropolymer compositions |
JP5044800B2 (ja) * | 2001-03-28 | 2012-10-10 | ダイキン工業株式会社 | 含フッ素エラストマー組成物 |
ITMI20011060A1 (it) | 2001-05-22 | 2002-11-22 | Ausimont Spa | Composizioni fluoroelastomeriche |
ITMI20011059A1 (it) | 2001-05-22 | 2002-11-22 | Ausimont Spa | Composizioni fluoroelastomeriche |
ITMI20011061A1 (it) | 2001-05-22 | 2002-11-22 | Ausimont Spa | Composizioni fluoroelastomeriche |
ITMI20011062A1 (it) | 2001-05-22 | 2002-11-22 | Ausimont Spa | Composizioni fluoroelastomeriche |
JP3873727B2 (ja) | 2001-12-04 | 2007-01-24 | ダイキン工業株式会社 | 含フッ素材料分散水性組成物、被覆物品製造方法及び被覆物品 |
US6921796B2 (en) | 2002-07-29 | 2005-07-26 | Illinois Tool Works, Inc. | Fluoroelastomer compositions, their preparation, and their use |
CN100513448C (zh) | 2002-12-23 | 2009-07-15 | 3M创新有限公司 | 具有含氮固化部位的氟塑料聚合物 |
US7247749B2 (en) | 2003-01-29 | 2007-07-24 | Greene, Tweed Of Delaware, Inc. | Bisaminophenyl-based curatives and amidine-based curatives and cure accelerators for perfluoroelastomeric compositions |
JP2006516671A (ja) | 2003-01-29 | 2006-07-06 | グリーン, ツイード オブ デラウェア, インコーポレイテッド | ペルフルオロエラストマー組成物のためのビスアミノフェニルベースの硬化剤および硬化促進剤ならびにアミジンベースの硬化剤および硬化促進剤 |
US20050107544A1 (en) | 2003-11-13 | 2005-05-19 | Shuhong Wang | Plasma resistant curable fluoroelastomer composition |
US7514506B2 (en) | 2004-03-31 | 2009-04-07 | Greene, Tweed Of Delaware, Inc. | Fast curing fluoroelastomeric compositions, adhesive fluoroelastomeric compositions and methods for bonding fluoroelastomeric compositions |
KR101206666B1 (ko) | 2004-05-20 | 2012-11-29 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 퍼플루오로엘라스토머 및 플루오로플라스틱의 블렌드 |
US7354974B2 (en) | 2004-05-20 | 2008-04-08 | Dupont Performance Elastomers Llc | Blends of perfluoroelastomers and fluoroplastics |
JP4778782B2 (ja) | 2004-12-28 | 2011-09-21 | ニチアス株式会社 | シール材 |
JP5029359B2 (ja) | 2005-05-02 | 2012-09-19 | ダイキン工業株式会社 | 架橋性ポリテトラフルオロエチレン組成物、ポリテトラフルオロエチレン架橋体粉末、ポリテトラフルオロエチレン成形体、樹脂ブレンド組成物、および樹脂ブレンド成形体 |
US20060270780A1 (en) | 2005-05-25 | 2006-11-30 | Ping Xu | High purity perfluoroelastomer composites and a processes to produce the same |
JP2007002150A (ja) | 2005-06-27 | 2007-01-11 | Nichias Corp | エラストマー成形体並びにこれを使用したゴム材料及びoリング |
US7294677B2 (en) | 2005-08-25 | 2007-11-13 | 3M Innovative Properties Company | Catalyst for making fluoroelastomer compositions and methods of using the same |
JP5162818B2 (ja) | 2005-11-17 | 2013-03-13 | ユニマテック株式会社 | 含フッ素共重合体ブレンド物 |
RU2319717C1 (ru) | 2006-07-10 | 2008-03-20 | Федеральное государственное унитарное предприятие "Научно-исследовательский институт синтетического каучука имени академика С.В. Лебедева" | Композиция на основе сополимера тетрафторэтилена и перфторалкилвиниловых эфиров |
JP2008266368A (ja) * | 2007-04-16 | 2008-11-06 | Daikin Ind Ltd | 含フッ素エラストマー組成物およびそれからなるシール材 |
US10023722B2 (en) | 2008-04-08 | 2018-07-17 | Greene, Tweed Technologies, Inc. | Oxygen plasma-resistant composition characterized by low sticking, and related methods |
JP2012512311A (ja) | 2008-12-17 | 2012-05-31 | グリーン, ツイード オブ デラウェア, インコーポレイテッド | チタン酸バリウムフィラー含有パーフルオロエラストマー組成物 |
WO2010076876A1 (en) | 2008-12-29 | 2010-07-08 | Daikin Industries, Ltd. | Perfluoroelastomer composition and crosslinked molded article made by crosslinking and molding said perfluoroelastomer composition |
JP5553320B2 (ja) | 2008-12-29 | 2014-07-16 | ダイキン工業株式会社 | 架橋性含フッ素エラストマー組成物および該組成物から作製された成形品 |
US20120100379A1 (en) * | 2010-10-20 | 2012-04-26 | Greene, Tweed Of Delaware, Inc. | Fluoroelastomer bonding compositions suitable for high-temperature applications |
-
2011
- 2011-09-20 US US13/237,884 patent/US9018309B2/en active Active
- 2011-09-20 JP JP2013530238A patent/JP5833657B2/ja active Active
- 2011-09-20 SG SG2013020961A patent/SG188623A1/en unknown
- 2011-09-20 EP EP11827389.5A patent/EP2619267A4/en not_active Withdrawn
- 2011-09-20 WO PCT/US2011/052424 patent/WO2012040250A2/en active Application Filing
- 2011-09-20 KR KR1020137008930A patent/KR101710748B1/ko active IP Right Grant
- 2011-09-23 TW TW100134302A patent/TWI563005B/zh active
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EP2619267A2 (en) | 2013-07-31 |
WO2012040250A2 (en) | 2012-03-29 |
US20120077935A1 (en) | 2012-03-29 |
JP2014502284A (ja) | 2014-01-30 |
KR101710748B1 (ko) | 2017-02-27 |
US9018309B2 (en) | 2015-04-28 |
JP5833657B2 (ja) | 2015-12-16 |
TW201219417A (en) | 2012-05-16 |
EP2619267A4 (en) | 2015-05-13 |
TWI563005B (en) | 2016-12-21 |
WO2012040250A3 (en) | 2014-04-03 |
KR20130117769A (ko) | 2013-10-28 |
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